Substituted organopolysiloxanes and use thereof

ABSTRACT

The present invention provides a compound of Formula 1: 
                         
The compound of Formula 1 is useful as a scavenger for the removal of unwanted organic and inorganic compounds, for solid phase extraction, for solid phase synthesis, for the immobilization of bio-molecules, as ion exchanger materials, as catalysts and catalyst supports and as chromatography materials.

The invention relates to new organopolysiloxanes and their use, forexample as catalysts, cation and anion exchangers, organic and inorganiccompound scavengers, solid phase purification or extraction materials,immobilisation materials for bio-molecules, anti-microbial agents,hydrophilicity modifiers, flameproofing agents, antistatic agents,biomedical devices, water repellent films and coatings, solid phasesynthesis materials and chromatography materials. The invention alsorelates to precursors of these new products and processes for theirproduction.

The use of functionalised solids is growing rapidly for many differentapplications such as solution phase synthesis, solid phase synthesis,solid phase extraction, catalysis, catalyst supports, productpurification and the immobilisation of bio-molecules. In theseapplications the advantages of functionalised solids are ease ofmanipulation, simple separation from the rest of the medium byfiltration and regeneration and reuse. Key requirements for thesefunctionalised solids are excellent physical and chemical stability overa wide range of operating conditions, broad solvent applicability, fastkinetics—fast and easy access to the functional groups and functionalgroups with high intrinsic activity for the desired application. Inaddition the preparation of these functionalised materials has to besimple from readily available reagents. Finally it is highlyadvantageous if the functional groups can be readily transformed intodifferent functionalised materials that can be used for otherapplications.

Substituted polystyrene derivatives are an important class of materialsbeing used for a range of applications. The chemical and physicalproperties of a variety of such polystyrene based systems are describedin the Bio-Rad Life Science Research Products catalogue 1998/99, pages56-64. However the physical and chemical properties of these polystyreneresins may possess disadvantages, for example poor chemical stabilityand thermal stability, believed to be due to the organic polymericbackbone. Additional problems for example swelling and shrinking inorganic solvents as well as the production of highly coloured unwantedside products may also be encountered. Generally, due to their poorthermal stability, these polystyrene resins cannot be used for anylength of time above 80° C., thus limiting their general applicability.In addition a range of chemical functionality cannot be readily attachedto these organic polymers due to the physical limitations of thesepolymers and the range of chemistry that can be used to attachéfunctional groups onto the aromatic rings.

Inorganic polymer systems such as silica, aluminium oxide and titaniumoxide have also been disclosed as functionalised materials. Activefunctional groups or metals can be attached by a variety of means tothese systems. However a number of problems may be encountered where thefunctional groups are only physically adsorbed for example lowfunctional group loading along with limitations in the range of solventsthat can be used and removal of the functional groups on use or onstanding. This is believed to be due to the rather weak attachmentbetween the functional group and the surface atoms on the support.Building the functional group into the framework may provide a morerobust material and may also permit higher functional group loadings.However in this approach there is a significant lack of readilyavailable starting materials as well as precursors for preparing suchstarting materials. In addition there are limited syntheticmethodologies for the preparation of suitable starting materials fromavailable precursors. A need exists to provide new synthetic methods aswell as starting compounds in order to make such functionalisedmaterials.

In solution phase organic synthesis functionalised solid materials areused to aid rapid purification and workup. Here these functionalisedsolid materials, also known as scavengers, can remove excess reagentsand side products. At the end of the reaction the scavenger is added toquench and selectively react with excess or unreacted reagents andreaction side products. The unwanted chemicals now attached to thefunctionalised materials are removed by simple filtration. This simpleprocess circumvents the standard purification methodologies ofliquid-liquid extraction, chromatography and crystallisation.Substituted polystyrene derivatives are the main class of materialsbeing used as scavengers. However as described above these materialssuffer a number of significant limitations such as lack of thermalstability (stable up to 80° C.), swelling and shrinking in organicsolvents and a limited range of functional groups. In addition to theneed to remove unwanted chemicals from the desired product there is arequirement to separate closely related compounds. For example theseparation of primary amines from secondary or secondary amines fromtertiary amines is a particular requirement in both the fine chemicaland pharmaceutical industries.

In solid phase synthesis substituted polystyrene derivatives are themain class of materials being used and likewise these materials sufferthe same limitations as described above. The use of functionalisedsilica materials for this application is limited by the availability ofsuitable functionalised materials.

Catalysts are utilised in the chemical and biochemical industry toconduct a wide range of chemical transformations. A range of homogenousand heterogeneous catalysts are used some of which require hightemperatures to be effective and some produce considerable amount ofbi-products and waste. These unwanted products and waste have to betreated and destroyed. The drive for more environmentally friendlyprocesses—Green Chemistry—highlights the need for reusable, moreeffective and selective catalysts. Examples of catalysts currently usedextensively across manufacturing industries include mineralacids—sulphuric acid, hydrochloric acid, hydrogen fluoride, phosphoricacid—Lewis acids—aluminium trichloride, boron trifluoride and zincchloride—and oxidation reagents—permanganate, manganese dioxide andchromium (VI). Catalysts, particularly solid phase catalysts, suitablyhave one or more of the following characteristics; good thermalstability, good chemical stability, flexibility to tailor the loading offunctional groups to optimise yield and selectivity, they do not swellto a material extent, ease of regeneration and good catalyst life. Thisneed has led to investigations into the design of new materials that caneither catalyse a variety of chemical transformations or be used as acatalyst solid support. In the latter the catalysts are firmly attachedonto functional groups that are strongly attached onto a stable support.

Key requirements for such new catalysts and catalyst supports are verygood thermal stability, high insensitivity to chemical attack, highfunctional group loading, fixed and rigid structures, optimum functionalgroups so as to avoid rearrangements and side products, limited swellingcapability, insolubility in organic solvents, ease of purification andhigh reusability, high ageing resistance and ease of access to thefunctional group which conducts the chemical transformation. In additionthe processes to make such catalyst systems and catalyst supports haveto be flexible so as to enable the production of optimum structures andshapes for specific reactions. This could include tailoring the porosityfrom anywhere between macroporous to microporous structures, variableloading of the functional group, ease of making different metalderivatives and selective pH ranges. Of particular interest for newcatalysts and catalyst supports are functional groups such as carbonyland carboxy due to their ease of manipulation and their capabilities tobind to metal complexes.

A range of metals and catalysts have been embedded within or adsorbed onto the surface of silica, and other materials These systems may sufferthe drawback of loss of the active functional groups due to their oftenvery weak attachment to the silica. A need remains for organo-silicamaterials which whilst retaining the appropriate function havefunctional groups that are strongly attached to the support and whichbind strongly to a range of metals and catalysts and do not catalyseother reactions to an undesirable extent which may lead to impure andhighly coloured products and lower yield and selectivity.

As a consequence of stricter environmental regulations there is agrowing requirement for more effective systems for the removal andrecovery of cations and anions from many sources including a widespectrum of contaminated solvents and aqueous based wastes and fromcontaminated waters. For example the electronics industry has aparticular need for ultra pure water with very low levels of bothcations and anions. Other industries such as the nuclear industry andthe electroplating industry generate substantial quantities ofwater-based effluent that are heavily contaminated with undesirablemetal ions. Cation exchangers have been used to remove metal ions fromsolution. Polymers having an organic partly cross-linked polystyrenebackbone with sulfonate groups attached to some of the phenyl rings areknown for use in this application and have certain drawbacks as regardsphysical and chemical properties of these polystyrene sulfonic cationexchangers are strongly affected by the organic nature of the polymericbackbone so that a number of disadvantages affect their technical fieldof application as noted above. The type of cation exchangers employed,consist primarily of an organic, partly cross-linked polystyrenebackbone with sulfonate groups attached to some of the phenyl rings. Thephysical and chemical properties of these polystyrene sulfonic cationexchangers are strongly affected by the organic nature of the polymericbackbone so that a number of disadvantages affect their technical fieldof application. Organophosphonic acid cation exchangers have also beenreported in U.S. Pat. No. 5,281,631 and U.S. Pat. No. 5,449,462. Thefeedstock in the manufacture of these materials may be expensive andthey have limited applicability due to their physical and chemicalproperties.

The invention relates to novel compounds which have a wide range of usesincluding acting as scavengers for inorganic and organic compounds,solid phase extraction and purification material, bio-moleculeimmobilisation supports, ion exchanger materials, as anti-microbialagents and as chromatography materials, as catalysts and catalystsupports or which are precursors for these.

In a first aspect of the present invention, there is provided a compoundof General Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is selected fromoxygen, hydrogen, OH, NR² and NNR²R³, and wherein X and Y are eachselected from hydrogen, —C(Z)R, CN or C(O)W and W is selected from OH,OR⁶, O(M^(+n))_(1/n), and NR²R³ and R, R¹, R², R³ and R⁶ are eachselected from hydrogen, an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-40-alkynyl group,an aryl and C₁₋₄₀-alkylaryl group and M is a metal ion derived from alanthanide, actinide, main group or transition metal and V is selectedfrom an optionally substituted linear or branched group selected fromC₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, an aryl group, aC₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, a polyalkyl amine,a phosphine or other phosphorous containing group; n is an integer from1 to 4;

the free valences of the silicate oxygen atoms are saturated by one ormore of:

silicon atoms of other groups of Formula 1, hydrogen, a linear orbranched C₁₋₁₂-alkyl group, by end groups R⁴ ₃M¹O_(1/2), bycross-linking bridge members R⁴ _(q)M¹(OR⁵)_(m)O_(k/2),Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2) or by chains, for examplepolymeric chains, comprising (R⁴ _(e)SiO_(f/2))_(g);

-   -   where M¹ is Si or Ti; e is an integer from 2 to 3 and f is an        integer from 1 to 2 such that e+f=4 and g is an integer from 1        to 10⁸, preferably from 1 to 100;        R⁵ is a linear or branched C₁₋₄₀, preferably C₁₋₁₂-alkyl group,        an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linear or branched        C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group;        k is an integer from 1 to 3 and q and m are integers from 0 to        2;        such that m+k+q=4;        p is an integer from 1 to 3; and r is an integer from 1 to 2;        or other known oxo metal bridging systems where the metal is        zirconium, boron, magnesium, iron, nickel or one of the        lanthanides; wherein both B and C are always present and the        integers a, b, c and d are such that the ratio of b:a+c+d is        from 0.00001 to 100,000.

Where a cross linker or polymer chain is used, it is preferred that theratio of end groups and/or cross linker and/or polymer chains to a+b+c+dvaries from 0 to 999:1 and preferably 0.001 to 999:1.

General Formula 1 may be abbreviated to A_(a)B_(b)C_(c)D_(d) where Arepresents [O_(3/2)SiCH(CH₂Q))CH₂CH₂SiO_(3/2)], B represents[O_(3/2)SiCH₂CH₂Q], C represents [O_(4/2)Si] and D represents[O_(3/2)SiV].

One advantage of compounds of Formula 1 is that the functional group orgroups can be selected to have either a high or low value according tothe application. Compounds of Formula 1 are advantageous in a number ofapplications including as catalysts, catalyst immobilisation supports,organic compound scavengers, solid phase purification and extractionmaterial, bio-molecule immobilisation supports, cation and anionexchanger materials, anti-microbial agents and chromatography materials.Other advantages include high thermal stability, fixed and rigidstructures, good stability to a wide range of chemical conditions,insolubility in organic solvents, high resistance to ageing, easilypurified and high reusability. In addition the processes for thepreparation of compounds of Formula 1 are very flexible, enablingporosity to be tailored from micro to macro porous, the loading of thefunctional groups X and Y as well as the other substituents in thefragment V to be varied as needed for example to provide high loading offunctional groups if required and a wide range of metal derivatives tobe made with the added advantage of a high metal incorporation.

The organic groups R, R¹, R², R³, R⁴, R⁵ and R⁶ may independently besubstituted with one or more substituents but preferably contain onlyhydrogen and carbon atoms. If a substituent is present, it may beselected from nitro, chloro, fluoro, bromo, nitrile, hydroxyl,carboxylic acid carboxylic esters, sulfides, sulfoxides, sulfones,C₁₋₆-alkoxy, a C₁₋₄₀-alkyl or aryl di substituted phosphine, amino,amino C₁₋₄₀-alkyl or amino di(C₁₋₄₀-alkyl) or C₁₋₄₀-alkyl phosphinic orphosphonic group. The organic groups R, R¹, R², R³, R⁴, R⁵ and R⁶ may,independently be linear or branched as desired.

Each organic group R, R¹, R², R³, R⁴, R⁵ and R⁶ is selectedindependently of any of the other organic groups in the compound ofFormula 1. Preferably, the organic groups R, R¹, R², R³, R⁴, R⁵ and R⁶are independently selected from linear or branched C₁₋₂₂ and desirablyC₁₋₁₂ alkyl, C₂₋₂₂- and desirably C₂₋₁₂ alkenyl, aryl and aC₁₋₂₂-alkylaryl group and especially preferred that the organic group R,R¹, R², R³, R⁴, R⁵ and R⁶ are independently selected from a linear orbranched C₁₋₈ alkyl, C₂₋₈-alkenyl, aryl and a C₁₋₈-alkylaryl group.

Suitably, R, R¹, R², R³, R⁴, R⁵ and R⁶ are independently a C₁₋₁₂-alkylgroup for example methyl or ethyl, or a phenyl group. Preferably q isfrom 1 to 2, k is from 1 to 3 and m is 0 provided that m+k+q=4.

Examples of suitable alkyl groups include methyl, ethyl, isopropyl,n-propyl, butyl, tert-butyl, n-hexyl, n-decyl, n-dodecyl, cyclohexyl,octyl, iso-octyl, hexadecyl, octadecyl, iso-octadecyl and docosyl.Examples of suitable alkenyl groups include ethenyl, 2-propenyl,cyclohexenyl, octenyl, iso-octenyl, hexadecenyl, octadecenyl,iso-octadecenyl and docosenyl.

C₁₋₆-alkoxy refers to a straight or branched hydrocarbon chain havingfrom one to six carbon atoms and attached to an oxygen atom. Examplesinclude methoxy, ethoxy, propoxy, tert-butoxy and n-butoxy.

The term aryl refers to a five or six membered cyclic, 8-10 memberedbicyclic or 10-13 membered tricyclic group with aromatic character andincludes systems which contain one or more heteroatoms, for example, N,O or S. Examples of suitable aryl groups include phenyl, pyridinyl andfuranyl. Where the term “alkylaryl” is employed herein, the immediatelypreceding carbon atom range refers to the alkyl substituent only anddoes not include any aryl carbon atoms. Examples of suitable alkarylgroups include benzyl, phenylethyl and pyridylmethyl.

Compounds in which Q is —C(Z)R and Z is selected from oxygen, OH,hydrogen, NR² and NNR²R³ and R is C₁₋₁₂-alkyl, preferably C₄₋₁₂-alkyl,phenyl or C₁₋₈-alkylaryl and V is vinyl, C₁₋₄-alkyl, phenyl orC₁₋₈-alkylaryl are especially preferred.

Compounds in which Q is CXYR.sup.1 wherein X and Y are eachindependently hydrogen, —C(Z)R, CN or C(O)W, Z is selected from oxygen,OH, hydrogen, NR² and NNR²R³ and W is selected from OH, OR⁶,O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ and R⁶ are eachindependently hydrogen, an optionally substituted linear or branchedC₁₋₈-alkyl, C₂₋₈-alkenyl, C₂₋₈-alkynyl group, an aryl or C₁₋₁₂-alkylarylgroup and M is a metal ion derived from a lanthanide, actinide, maingroup or transition metal and n is an integer from 1 to 4; and V isvinyl, C₁₋₄-alkyl, phenyl or C₁₋₄-alkylaryl are also especiallypreferred.

Group Z may be either a divalent species for example a carbonyl oxygenor may comprise two monovalent species together, for example H and OH.

Where a cross linker is used, it is preferred that the ratio of crosslinker or polymer chains to a+b+c+d varies from 0 to 99:1 and preferably0.01 to 99:1. Particularly suitable cross linkers, end groups or polymerchains are derived from titanium alkoxides, aluminium trialkoxides andalkyl alkoxy silanes. Examples of cross linkers include aluminiumtriethoxide, aluminium tributoxide and titanium isopropoxide and forpolymer chains alkyl alkoxy silanes. The end group, cross linking bridgeor polymer chain member is preferably (R⁴)₃SiO_(1/2) or (R⁴)₂SiO_(2/2)or TiO_(4/2) or R⁴TiO_(3/2) or (R⁴)₂TiO_(2/2) or AlO_(3/2) orR⁴AlO_(2/2). R⁴ is preferably C₁₋₄-alkyl or aryl, most preferably methylor ethyl or phenyl.

The preparation of compounds of Formula 1 will now be discussed ingreater detail. The general procedure used for the production of theorganopolysiloxanes of Formula 1 consists of first forming the compounds(R⁵O)₃SiCH₂CH₂Q or (R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ and (R⁵O)₃SiCH₂CH₂Q,and then combining them with tetraalkyl orthosilicate, (R⁵O)₄Si, aloneor with other compounds such as (R⁵O)₃SiV, titanium alkoxides, aluminiumtrialkoxides and alkyl alkoxy silanes, in the desired ratios, in solventwith either dilute acid or base. An alternative method for thepreparation of compounds of Formula 1 involves the treatment ofpreformed materials such as silica or aluminium oxide with(R⁵O)₃SiCH₂CH₂Q or (R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ and (R⁵O)₃SiCH₂CH₂Q togive the corresponding functionalised material.

Organopolysiloxanes of Formula 1 where X or Y or both X and Y containone or more carbonyl groups can be transformed into other materials ofFormula 1 containing either alcohol, amide or imine functional groupsvia reduction or through reaction with an amine or hydrazine.

It has been reported that substituted ketones, esters and nitriles canbe prepared through the free radical addition of aldehydes, esters ornirtiles to double bonds. This is described in Org. Reactions. Vol. 13,108. The majority of this work concerns the addition of aldehydes oresters to simply substituted olefins. Emphasis was primarily onunsubstituted C₂₋₁₆ olefins. For silicon containing olefins there areonly a small number of examples that include the reaction of butanalwith trimethyl vinylsilane reported in J. Amer. Chem. Soc., 1954, 76,1615 to give 1-(trimethylsilyl) hexan-3-one using benzoyl peroxide asthe free radical generator. Photochemical addition of aldehydes to vinylsilanes has been reported in Bull. Acad. Sci. USSR Div. Chem. Science1966, 1405 to give the corresponding ketone (RO)₃SiCH₂CH₂COR where R ismethyl, propyl and phenyl. Aqueous acid hydrolysis of(EtO)₃SiCH₂CH₂COCH₃ gave a soft polymer of formula[CH₃COCH₂CH₂SiO_(3/2)]_(n), that doesn't have the required physicalproperties for use as a solid material.

It is known that free radical reactions involving alkenes may notproceed in high yield or selectivity, depending on the particularstarting materials unwanted dimers and higher tellomers may undesirablybe produced, as disclosed in Org. Reactions, Vol. 13, page 218-222 andthe references provided therein. However there is a lack of simple andeffective synthetic methodology for the preparation of functionalisedorganic or inorganic polymers or materials. Furthermore there is asignificant lack of readily available starting materials as well asprecursors for preparing such starting materials. In addition there arelimited synthetic methodologies for the preparation of suitable startingmaterials from available precursors. Cross-linking may produce stablesolid polymer materials that otherwise would not have the requiredchemical and physical properties to be utilised. The present inventorshave found that the hitherto unwanted dimerisation and tellomerisation,in the radical addition to olefins, provides a means to prepare stablefunctionalised solid materials.

Compounds such as (R⁵O)₃SiCH₂CH₂Q or compounds(R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ and (R⁵O)₃SiCH₂CH₂Q were synthesised viaa free radical promoted addition of the corresponding precursor such asan aldehyde, ester or nitrile to vinyl trialkoxy silane. R⁵ is a linearor branched C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl or C₂₋₄₀-alkynyl group, aryl orC₁₋₄₀-alkylaryl group. The ratio of (R⁵O)₃SiCH₂CH₂Q to(R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ can be controlled through the relevantconcentrations of the starting materials trialkoxy vinyl silane to thealdehyde, ester or nitrile. High concentrations of the aldehyde, esteror nitrile to trialkoxy vinyl silane lead to high selectivity for(R⁵O)₃SiCH₂CH₂Q. Slow addition of the trialkoxy vinyl silane to excessof the aldehyde, ester or nitrile precursor also favours the preparationof (R⁵O)₃SiCH₂CH₂Q.

For example slow addition of vinyltriethoxy silane to ethyl cyanoacetate gave a mixture of (EtO)₃SiCH₂CH₂CH(CN)CO₂Et and(EtO)₃SiCH(CH₂CH(CN)CO₂Et)CH₂CH₂Si(OEt)₃. The ratio of these twocompounds is dependent on the relative ratio of the starting materials,vinyl triethoxy silane to ethyl cyano acetate. As the ratio of thelatter to the former increases then the ratio of the mono to bistrialkoxy silyl compound likewise increases. Using similar reactionconditions (EtO)₃SiCH₂CH₂CH(C(O)CH₃)CO₂Et and(EtO)₃SiCH(CH₂CH(C(O)CH₃)CO₂Et)CH₂CH₂Si(OEt)₃ were produced from vinyltriethoxy silane and ethyl acetoacetate. Likewise starting from vinyltriethoxy silane and dimethyl malonate (EtO)₃SiCH₂CH₂CH(C(O)OCH₃)₂ and(EtO)₃SiCH(CH₂CH(C(O)OCH₃)₂)CH₂CH₂Si(OEt)₃ were produced. From vinyltriethoxy silane and 2,4-pentadione (EtO)₃SiCH₂CH₂CH(C(O)CH₃)₂ and(EtO)₃SiCH(CH₂CH(C(O)CH₃)₂)CH₂CH₂Si(OEt)₃ were produced.

A wide range of free radical initiators can be used for this reactionand preferred are the peroxides and in particular the alkyl peroxides.Addition of a very small amount of the initiator every few hoursimproves the overall yield. Reaction temperatures between 60-170° C. canbe used, though a reaction temperature of between 100-140° C. ispreferred. Di-tert-butyl peroxide is the preferred free radicalinitiator. Reaction times of between 15 minutes to 48 hours have beenused with 6 to 18 hours preferred. On completion the unreacted startingmaterials are distilled off under reduced pressure and the resultantmixture is heated at between 100-120° C. at 1-2 mm of Hg. The unreactedstarting materials can be reused in the next batch.

Acids and bases were used to catalyse the hydrolysis of the siliconesters of (R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃, (R⁵O)₃SiCH₂CH₂Q and tetraalkyl orthosilicates to produce the organopolysiloxanes of Formula 1. M.A. Brook in Silicon in Organic, Organometallic and Polymer ChemistryChapter 10, page 318, John Wiley & Sons, Inc., 2000, G. A. Scherer inSol-gel science: the physics and chemistry of sol-gel processing,Boston: Academic Press, 1990, and J. D. Wright in Sol-gel materials:chemistry and applications, Amsterdam: Gordon & Breach SciencePublishers, 2001 and the references contained within describe sol-geltechnology and the hydrolysis of silicon esters.

A range of solvents, known to those skilled in the art of organicchemistry, can be used to conduct this reaction. Alcohols are thepreferred solvents particularly methanol and ethanol. After standing fora period of time the solution can be warmed to speed up the formation ofthe glass. Ratios from 100 to 0.01, by weight, of the alcohol solvent tothe combined weight of the reagents can be used, with ranges from 2-10being preferred. A range of acids may be used to aid hydrolysis withhydrochloric acid in concentrations ranging from 0.1 to 4 M beingpreferred. Hydrochloric acid, 1 molar, is especially preferred. Ratios,from 0.0001 to 10, of hydrochloric acid, 1 molar, to the combined weightof the reagents are suitably be used, with a ratio from 0.01 to 1 beingpreferred. The reaction mixture may be left to stand at a temperature inthe range 0° C.-120° C. to aid hydrolysis and the formation of theSi—O—Si bonds. Temperatures between 20-90° C. are preferred and suitablywarming is continued until all the solvent has evaporated and a clearglass is obtained.

Compounds containing A, B, C and D, fragments were prepared through anidentical sol gel process using the precursors (R⁵O)₃SiCH₂CH₂Q,(R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃, (R⁵O)₃SiV and tetraalkyl orthosilicate.

In addition to (R⁵O)₃SiCH₂CH₂Q, (R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃,(R⁵O)₃SiV and tetraalkyl orthosilicate, precursors to end groups,cross-linking bridge members or polymer chains such as R⁴SiO_(3/2) or(R⁴)₂SiO_(2/2) or TiO_(4/2) or R⁴TiO_(3/2) or (R⁴)₂TiO_(2/2) orAlO_(3/2) or R⁴AlO_(2/2), where R⁴ is as defined above, but ispreferably methyl, ethyl or phenyl can be added in varying ratios toproduce the desired compound of Formula 1. These end group, crosslinking bridge or polymer chain precursors are added at the same time ascompounds (R⁵O)₃SiCH₂CH₂Q, (R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃, (R⁵O)₃SiV andtetraalkyl orthosilicate.

Templates to aid the preparation of pores with particular sizes anddistributions in compounds of Formula 1 can also be added at thisparticular stage. On preparation of the solid organopolysiloxanes ofFormula 1 these templates can be washed out.

Compounds of Formula 1 can also be prepared by treating a preformedmaterial such as silica or aluminium oxide with (R⁵O)₃SiCH₂CH₂Q, or with(R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ and (R⁵O)₃SiCH₂CH₂Q, or with(R⁵O)₃SiCH₂CH₂Q, (R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ and, (R⁵O)₃SiV invarying ratios in a solvent.

Compounds of Formula 1 have a wide range of uses. The present inventionprovides a process for treating a feed material comprising contacting acompound of Formula 1 with a feed material:

i) to effect a chemical reaction by catalytic transformation of acomponent of the feed material to produce a desired product;

ii) to remove a component of the feed material so as to produce amaterial depleted in the removed component; or

iii) to remove an ionic species in the feed material in an ion exchangeprocess.

The feed material may be a continuous stream for example a continuousprocess reaction feedstock, or may be in the form of a batch of materialfor discrete treatment. The feed material, for example a waste water orwaste process stream, may be treated to selectively remove a componentsof the feed. The removed component may be an undesirable material in thefeed and the process acts to provide a desired composition for the feedmaterial that has been depleted in the selectively removed componentafter contact with compounds of Formula 1. This process may be used forexample in removing unwanted species from a feed material in apharmaceutical manufacturing or formulation process to improve thepurity level of the pharmaceutical product as regards the removedmaterial, for example metal species.

The process may be employed to remove desired species from a feedmaterial for subsequent processing or analysis, for example a biologicalmolecule such as an enzyme, peptide, protein and nucleic acid may beremoved from a feed material to enable further processing or analysis ofthe removed components.

Compounds of Formula 1 can be used to remove excess reagents and sideproducts from reactions mixtures. The purification of primary, secondaryand tertiary amines is a common problem for the fine chemical andpharmaceutical industries. In particular the purification of a secondaryamine in the presence of a related primary amine is a common challenge.The carbonyl containing compounds prepared in Examples 2, 4, 5, 7, 9 and21 can readily remove primary amines and hydrazines from reactionmixtures. In addition these materials can selectively remove primaryamines in the presence of secondary and tertiary amines. The followingexamples illustrate the scavenging of unwanted organic and inorganiccompounds by compounds of Formula 1 but are not intended to limit thescope of their capability. Treatment of solutions containing primaryamines such as benzylamine, hexylamine and 3-methoxypropylamine with 2to 4 equivalents of organopolysiloxane ketones of Formula 1 at roomtemperature for 1 hour led to the complete removal of the amine. Withsecondary amines such as dibenzylamine no scavenging was observed evenwith large excesses of organopolysiloxane ketones of Formula 1. Excessborohydrides such as sodium borohydride can be removed on treatment withthe organopolysiloxane ketones of Formula 1, such as the products fromExamples 2, 4, 5, 16, 18, 19 and 21.

Unlike the polystyrene based scavengers, organopolysiloxane compounds ofFormula 1 can work in all solvents, do not suffer from swelling and arenot limited in their application to reaction temperatures below 80° C.

Compounds of Formula 1 can also be used for the separation or removal ofgases, including the removal of malodorous volatile organic compounds.For example the removal of malodorous amines can be achieved withcarboxylic acids prepared in Example 22.

Compounds of Formula 1 can also be used as catalysts and asheterogeneous supports for the immobilisation of catalysts. For examplea palladium catalyst formed in Example 24 is an efficient heterogeneouscatalyst for carbon bond formation reactions such as Suzuki and Heck, asillustrated in Example 34. These heterogeneous catalysts possess thesignificant advantages that they can be filtered from the reactionmedium and then recycled and reused. This circumvents the problemsencountered when homogeneous catalysts are used of significant loss ofexpensive and often toxic catalysts, catalyst inclusion in the reactionproducts and the separation of the catalyst from the reaction mixture.

Compounds of Formula 1 can also be used for the removal of cations andanions from water, waste streams, waste waters and potable water. Inaddition these compounds of Formula 1 can remove impurities such asmetal ions contained in chemical products. For example the product ofExample 23 can remove main group, transition, lanthanide and actinidemetal ions from such environments.

Compounds of Formula 1 can also be used for solid phase synthesisthrough first attachment of the starting material to the carbonyl group,a number of chemical reactions can then be conducted and in each steppurification is facile through simple filtration. At the end of thesequence the desired material is released from the solid phase. Inaddition compounds of Formula 1 can be used as materials for solid phaseextraction where a desired product is purified through selectiveretention on the functionalised materials whilst the impurities areremoved and then it is subsequently released.

Further applications of compounds of Formula 1 include the use asmaterials for chromatographic separations. For example the materials ofFormula 1 can be used in the separation of amines, including opticallyactive amines. Primary amines can be selectively separated fromsecondary amines using compounds of Formula 1.

Compounds of Formula 1 can be used as materials for gel filtration andhigh speed size-exclusion chromatography as well as for high pressureliquid chromatography and solid phase extraction.

Compounds of Formula 1 can be used both to immobilise biologicalmolecules such as enzymes, polypeptides, proteins and nucleic acids aswell as for their separation and purification. In addition nucleic acidsimmobilised on compounds of Formula 1 can be used for conducting highvolume nucleic acid hybridization assays.

Compounds of Formula 1 can be used as anti-microbial agents. Theinvention also provides an antimicrobial composition comprising acompound of Formula 1 and a carrier. Compounds of Formula 1 can beapplied as thin films onto a variety of surfaces.

The invention will now be described in detail with reference toillustrative examples of the invention.

EXAMPLE 1

A solution containing triethoxyvinylsilane (20.9 g, 0.11 mol) anddi-tert butyl peroxide (10 drops) was added dropwise to heptanal (68.71g, 0.60 mol) at 115° C. under an atmosphere of nitrogen over an hour.The solution was heated to 150° C. maintained at this temperature for 4h during which di-tert butyl peroxide (10 drops) was added every 20 min.The excess starting material was then removed under reduced pressure at120° C. to give (EtO)₃SiCH₂CH₂C(O)C₆H₁₃ and(EtO)₃SiCH(CH₂C(O)C₆H₁₃)CH₂CH₂Si(OEt)₃ as a pale yellow oil (32.8 g).¹³C NMR CDCl₃, 210 ppm C═O.

EXAMPLE 2

A mixture of the product from Example 1 (19.76 g) and tetraethylorthosilicate (84 g) was dissolved in methanol (160 cm³) and 1 M HCl (20cm³) was added with stirring. The mixture was then left in a water bathat 80° C. until the methanol had evaporated and a glass had formed. Theglass was crushed and stirred in refluxing methanol. The material wasdried to give a cream coloured powder. IR C═O at 1704 cm⁻¹.

EXAMPLE 3

A solution containing triethoxyvinylsilane (20.9 g, 0.11 mol) anddi-tert butyl peroxide (10 drops) was added dropwise to heptanal (102.71g, 0.9 mol) at 115° C. under an atmosphere of nitrogen over two hours.The solution was maintained at this temperature for 22 h during whichdi-tert butyl peroxide (10 drops) was added every 20 min. The excessstarting material was then removed under reduced pressure at 120° C.(EtO)₃SiCH₂CH₂C(O)C₆H₁₃ and (EtO)₃SiCH(CH₂C(O)C₆H₁₃)CH₂CH₂Si(OEt)₃ as apale yellow oil (31.8 g). ¹³C NMR CDCl₃, 210 ppm C═O.

EXAMPLE 4

A mixture of the product from Example 3 (5.76 g) and tetraethylorthosilicate (32.22 g) was dissolved in methanol (140 cm³) and 1 M HCl(20 cm³) was added with stirring. The mixture was then left in a waterbath at 80° C. until the methanol had evaporated and a glass had formed.The glass was crushed and then stirred in refluxing methanol. Thematerial was then dried under reduced pressure of 0.1 mm Hg at 50° C.for 2 h to give a cream coloured powder. IR C═O at 1704 cm⁻¹.

EXAMPLE 5

A mixture of the product from Example 1 (4.6 g) and tetraethylorthosilicate (32.69 g) was dissolved in methanol (140 cm³) and 1 M HCl(18 cm³) was added with stirring. The mixture was then left in a waterbath at 80° C. until the methanol had evaporated and a glass had formed.The glass was crushed and then stirred in refluxing methanol. Thematerial was then dried under reduced pressure of 0.1 mm Hg at 50° C.for 2 h to give a cream coloured powder. IR C═O at 1704 cm⁻¹.

EXAMPLE 6

A solution containing trimethoxyvinylsilane (16.76 g, 0.11 mol) anddi-tert butyl peroxide (10 drops) was added dropwise to octanal (76.93g, 0.60 mol) at 115° C. under an atmosphere of nitrogen over two hours.The solution was maintained at this temperature for 22 h during whichdi-tert butyl peroxide (10 drops) was added every 20 min. The excessstarting material was then removed under reduced pressure at 120° C. togive (MeO)₃SiCH₂CH₂C(O)C₇H₁₅ and (MeO)₃SiCH(CH₂C(O)C₇H₁₅)CH₂CH₂Si(OMe)₃a pale yellow oil (37.4 g). ¹³C NMR CDC₃, 210 ppm C═O.

EXAMPLE 7

A mixture of the product from Example 6 (9.46 g) and tetraethylorthosilicate (51.67 g) was dissolved in methanol (160 cm³) and 1 M HCl(20 cm³) was added with stirring. The mixture was then left in a waterbath at 80° C. until the methanol had evaporated and a glass had formed.The glass was crushed and then stirred in refluxing methanol. Thematerial was then dried under reduced pressure of 0.1 mm Hg at 50° C.for 2 h to give a cream coloured powder. IR C═O at 1704 cm³¹ ¹.

EXAMPLE 8

A solution containing trimethoxyvinylsilane (16.46 g, 0.11 mol) anddi-tert butyl peroxide (10 drops) was added dropwise to nonanal (85.34g, 0.60 mol) at 115° C. under an atmosphere of nitrogen over two hours.The solution was maintained at this temperature for 22 h during whichdi-tert butyl peroxide (10 drops) was added every 20 min. The excessstarting material was then removed under reduced pressure at 120° C. togive (MeO)₃SiCH₂CH₂C(O)C₈H₁₇ and (MeO)₃SiCH(CH₂C(O)C₈H₁₇)CH₂CH₂Si(OMe)₃as a pale yellow oil (39.2 g). ¹³C NMR CDCl₃, 210 ppm C═O.

EXAMPLE 9

A solution of the product from Example 8 (6.46 g) and tetraethylorthosilicate (41.67 g) was dissolved in methanol (160 cm³) and 1 M HCl(20 cm³) was added with stirring. The mixture was then left in a waterbath at 80° C. until the methanol had evaporated and a glass had formed.The glass was crushed and then stirred in refluxing methanol. Thematerial was then dried under reduced pressure of 0.1 mm Hg at 50° C.for 2 h to give a cream coloured powder. IR C═O at 1704 cm⁻¹.

EXAMPLE 10

A solution of the product from Example 1 (7.1 g) and tetraethylorthosilicate (41.3 g) and dimethoxy dimethyl silane (2.4 g) wasdissolved in methanol (160 cm³) and 1 M HCl (22 cm³) was added withstirring. The mixture was then left in a water bath at 80° C. until themethanol had evaporated and a glass had formed. The glass was crushedand then stirred in refluxing methanol. The material was then driedunder reduced pressure of 0.1 mm Hg at 50° C. for 2 h to give a creamcoloured powder. IR C═O at 1704 cm⁻¹.

EXAMPLE 11

A solution of the product from Example 1 (8.9 g) and tetraethylorthosilicate (41.3 g) and trimethoxy methyl silane (2.1 g) wasdissolved in methanol (160 cm³) and 1 M HCl (21 cm³) was added withstirring. The mixture was then left in a water bath at 80° C. until themethanol had evaporated and a glass had formed. The glass was crushedand then stirred in refluxing methanol. The material was then driedunder reduced pressure of 0.1 mm Hg at 50° C. for 2 h to give a creamcoloured powder. IR C═O at 1704 cm⁻¹.

EXAMPLE 12

A solution of the product from Example 1 (4.9 g) and tetraethylorthosilicate (41.3 g) and trimethoxy phenyl silane (1.8 g) wasdissolved in methanol (160 cm³) and 1 M HCl (21 cm³) was added withstirring. The mixture was then left in a water bath at 80° C. until themethanol had evaporated and a glass had formed. The glass was crushedand then stirred in refluxing methanol. The material was then driedunder reduced pressure of 0.1 mm Hg at 50° C. for 2 h to give a creamcoloured powder. IR C═O at 1706 cm⁻¹.

EXAMPLE 13

A solution containing triethoxyvinylsilane (19.0 g, 0.10 mol), ethylcyanoacetate (11.3 g, 0.1 mol) and di-tert butyl peroxide (10 drops) wasadded dropwise to ethyl cyanoacetate (67.8 g, 0.6 mol) at 150° C. underan atmosphere of nitrogen over two hours. The solution was maintained atthis temperature for 22 h during which di-tert butyl peroxide (10 drops)was added every 20 min. The excess starting material was then removedunder reduced pressure to give ethyl 2-cyano 4-triethoxysilyl butanateand ethyl 2-cyano 4, 6-di(triethoxysilyl) hexanoate as a pale yellow oil(26.8 g).

EXAMPLE 14

A solution of the product from Example 13 (6.83 g) and tetraethylorthosilicate (53 ml) was dissolved in methanol (160 cm³) and 1 M HCl(28 cm³) was added with stirring. The mixture was then left in a waterbath at 80° C. until the methanol had evaporated and a glass had formed.The glass was crushed and then stirred in refluxing methanol. Afterfiltration the material was then dried under reduced pressure of 0.1 mmHg at 50° C. for 2 h to give a cream coloured powder where in Formula 1Q is CXYR¹ and X═CN, Y═CO₂Et, R¹=hydrogen, ratio a+b:c=1:0 and d=0.

EXAMPLE 15

A solution containing triethoxyvinylsilane (19.0 g, 0.10 mol), 2,4pentadione (6.5 g) and di-tert butyl peroxide (10 drops) was addeddropwise to 2,4 pentadione (56.5 g, 0.565 mol) at 150° C. under anatmosphere of nitrogen over two hours. The solution was maintained atthis temperature for 22 h during which di-tert butyl peroxide (10 drops)was added every 20 min. The excess starting material was then removedunder reduced pressure to give 3-acetyl 5-triethoxysilyl pentan-2-oneand 3-acetyl 5,7-di(triethoxysilyl) heptan-2-one as a pale yellow oil(25.8 g).

EXAMPLE 16

A solution of the product from Example 15 (6.2 g) and tetraethylorthosilicate (53 ml) was dissolved in methanol (160 cm³) and 1 M HCl(28 cm³) was added with stirring. The mixture was then left in a waterbath at 80° C. until the methanol had evaporated and a glass had formed.The glass was crushed and then stirred in refluxing methanol. Afterfiltration the material was then dried under reduced pressure of 0.1 mmHg at 50° C. for 2 h to give a cream coloured powder where in Formula 1Q is CXYR¹ and X═C(O)Me, Y═C(O)Me, R¹=hydrogen, ratio a+b:c=1:10 andd=0.

EXAMPLE 17

A solution containing triethoxyvinylsilane (22.0 g), ethyl acetoacetate(14.2 g) and di-tert butyl peroxide (3 ml) was added dropwise to 2,4pentadione (56.5 g, 0.565 mol) at 150° C. under an atmosphere ofnitrogen over two hours. The solution was maintained at this temperaturefor 22 h during which di-tert butyl peroxide (10 drops) was added every20 min. The excess starting material was removed under reduced pressureto give ethyl 3-acetyl 5-triethoxysilyl butanate and 3-acetyl 5,7di(triethoxysilyl) hexanate as a pale yellow oil (30.8 g).

EXAMPLE 18

A solution of the product from Example 17 (6.2 g) and tetraethylorthosilicate (52 ml) was dissolved in methanol (160 cm³) and 1 M HCl(28 cm³) was added with stirring. The mixture was then left in a waterbath at 80° C. until the methanol had evaporated and a glass had formed.The glass was crushed and then stirred in refluxing methanol. Afterfiltration the material was then dried under reduced pressure of 0.1 mmHg at 50° C. for 2 h to give a cream coloured powder where in Formula 1Q is CXYR¹ and X═C(O)Me, Y═C(O)OEt, R¹=hydrogen, ratio a+b:c=1:10 andd=0.

EXAMPLE 19

Silica (20 g, 60-200 μm) was added to a solution of the product fromExample 17 (6.2 g) in toluene (80 ml) and the resultant mixture wasstirred under gentle reflux for 4 h. The solid was filtered and washedwell with methanol and dried under reduced pressure to give a creamcoloured powder where in Formula 1 Q is CXYR¹ and X═C(O)Me, Y═C(O)OEt,R¹=hydrogen, ratio a+b:c=1:10 and d=0.

EXAMPLE 20

Silica (20 g, 60-200 μm) was added to a solution of the product fromExample 13 (7.2 g) in toluene (80 ml) and the resultant mixture wasstirred under gentle reflux for 4 h. The solid was filtered and washedwell with methanol and dried under reduced pressure to give a creamcoloured powder where in Formula 1 Q is CXYR¹ and X═CN, Y═CO₂Et,R¹=hydrogen, ratio a+b:c=1:10 and d=0.

EXAMPLE 21

Silica (20 g, 60-200 μm) was added to a solution of the product fromExample 1 (7.2 g) in toluene (80 ml) and the resultant mixture wasstirred under gentle reflux for 4 h. The solid was filtered and washedwell with methanol and dried under reduced pressure to give a creamcoloured powder where in Formula 1 Q is CXYR¹ and X=hydrogen, Y═COC₆H₁₃,R¹=hydrogen, and d=0.

EXAMPLE 22

A mixture containing the product from Example 19 (5 g) and hydrochloricacid (3M, 40 ml) was refluxed with stirring for 4 h and then cooled toroom temperature. The solid was filtered and washed well with methanoland dried under reduced pressure to give a cream coloured powder wherein Formula 1 Q is CXYR¹ and X═C(O)Me, Y═C(O)OH, R¹=hydrogen, ratioa+b:c=1:10 and d=0.

EXAMPLE 23

A mixture of the product from Example 22 (1.0 g) in water (30 ml) wastreated with an aqueous solution of sodium hydroxide until the pH was 7.The white solid was filtered, washed well with distilled water andfinally with methanol. The material was then dried under reducedpressure of 0.1 mm Hg at 80° C. for 2 h to give the sodium carboxylatesalt of Example 22 as a white powder (0.9 g).

EXAMPLE 24

A solution of palladium acetate (0.20 g) in THF (50 ml) was added to thesodium salt of the carboxylic acid (Example 23, 2.0 g) and the mixturewas stirred overnight. The yellow solid was filtered and washed wellwith THF and then dried.

EXAMPLE 25

A mixture of anisole (0.03585 g, 0.33 mmol) as a marker, benzylamine(0.04047 g, 0.38 mmol) and the product from Example 2 (0.48685 g, 1.51mmol) was stirred in CDCl₃ (2.5 cm³) at room temperature for 1 h. Themixture was then centrifuged and a ¹H NMR spectrum of the chloroformsolution showed that the benzylamine was completely removed.

EXAMPLE 26

A mixture of anisole (0.02860 g, 0.26 mmol), hexylamine (0.02504 g, 0.25mmol) and the product from Example 2 (0.32297 g, 1.0 mmol) was stirredin CDCl₃ (2.5 cm³) at room temperature for 1 h. The mixture was thencentrifuged and a ¹H NMR spectrum of the chloroform solution showed thatthe hexylamine was completely removed.

EXAMPLE 27

A mixture of anisole (0.03415 g, 0.32 mmol), 3-methoxypropylamine(0.02901 g, 0.33 mmol) and the product from Example 2 (0.42552 g, 1.32mmol) was stirred in CDCl₃ (2.5 cm³) at room temperature for 1.5 h. Themixture was then centrifuged and a ¹NMR spectrum of the chloroformsolution showed that the 3-methoxypropylamine was completely removed.

EXAMPLE 28

A mixture of dimethoxyethane (0.03580 g, 0.40 mmol) as a marker,dibenzylamine (0.03850 g, 0.19 mmol) and the product from Example 2(0.25134 g, 0.78 mmol) was stirred in CDCl₃ (2.5 cm³) at roomtemperature for 1 h. The mixture was then centrifuged and a ¹H NMRspectrum of the chloroform solution showed that the secondary aminedibenzylamine had not been removed.

EXAMPLE 29

A mixture of anisole (0.034 g, 0.32 mmol), hydrazine hydrate (0.015 g,0.30 mmol) and the product from Example 2 (0.42 g, 1.32 mmol) wasstirred in CDCl₃ (2.5 cm³) at room temperature for 1.5 h. The mixturewas then centrifuged and a ¹H NMR spectrum of the chloroform solutionshowed that the hydrazine was completely removed.

EXAMPLE 30

A mixture of dimethoxyethane (0.02304 g, 0.26 mmol), phenylhydrazine(0.03322 g, 0.31 mmol) and the product from Example 2 (0.39570 g, 1.23mmol) was stirred in CDCl₃ (2.5 cm³) at room temperature for 1 h. Themixture was then centrifuged and a ¹H NMR spectrum of the chloroformsolution showed that the phenylhydrazine was completely removed.

EXAMPLE 31

The ketone from Example 2 (2.03 g) was added to a methanolic solution ofsodium borohydride (1.19 g) and stirred for 4 h. The mixture wasfiltered and the solid was washed well with water and then withmethanol. IR C═O, peak at 3550 cm⁻¹ and no peak at 1702 cm⁻¹.

EXAMPLE 32

Hydrazine hydrate was added to a mixture of the ketone from Example 2(2.23 g) in methanol (15 ml). The mixture was then stirred for 1 h andthen filtered. The solid was washed well with methanol and then dried togive the corresponding imine.

EXAMPLE 33

A mixture of the palladium catalyst formed in Example 24 (50 mg),4-bromotoluene (1.6 mmol), phenyl boronic acid (1.6 mmol) and potassiumcarbonate (2.4 mmol) in xylene (10 ml) was warmed at 110° C. withstirring for 1 hour. The mixture was filtered and the solid washed withether. The combined organic extracts were washed with water, dried andthen concentrated to give 4-methyl biphenyl in 99% yield. The filteredsolid was returned to the reaction flask and further 4-bromotoluene (1.6mmol), phenyl boronic acid (1.6 mmol) and potassium carbonate (2.4 mmol)in xylene (10 ml) was added and the process repeated to give 4-methylbiphenyl in 99% yield.

EXAMPLE 34

The product from Example 24 (0.2 g) was added to a sample (2 ml) of asolution of ferric (III) chloride (1000 ppm) in water. The mixture wasstirred for 1 h at room temperature and then filtered. Analysis of thefiltrate showed that ferric chloride had been removed.

The invention claimed is:
 1. A compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2, such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula
 1. 2. The compound asclaimed in claim 1 which is selected from one or more end groups, crosslinking bridge members or polymer chains and wherein the molar ratio ofend group, cross linker and/or chain to a+b+c+d is from 0.001 to 999:1.3. The compound as claimed in claim 1 that is selected from an end groupselected from a trialkyl or triaryl alkoxysilane, or a cross linkingbridge member derived from an orthosilicate, a titanium alkoxide or aaluminium trialkoxide or a polymer chain selected from a mono alkyl ormono aryl trialkoxysilane or a di alkyl or di aryl dialkoxysilane. 4.The compound as claimed in claim 3 wherein the one or more end groups orcross-linking bridges or polymer chains are selected from R⁴ ₃SiO_(1/2),R⁴ ₂SiO_(2/2), TiO_(4/2), R⁴TiO_(3/2), R⁴ ₂TiO_(2/2), AlO_(3/2) andR⁴AlO_(2/2).
 5. The compound as claimed in claim 4 wherein R⁴ is aC₁₋₄-alkyl, C₂₋₁₂-alkenyl or aryl group.
 6. The compound as claimed inclaim 1 wherein Z is divalent and selected from oxygen, NR² and NNR²R³or comprises OH and H, and R, where —C(Z)R is present, and R¹, whereCXYR¹ is present, are each selected from an optionally substitutedC₁₋₂₀-alkyl, C₂₋₁₂-alkenyl, C₂₋₁₂-alkynyl, aryl, C₁₋₈-alkylaryl groupand R², R³ and R⁶ are each selected from an optionally substitutedC₁₋₁₂-alkyl, C₂₋₁₂-alkenyl, C₂₋₁₂-alkynyl, aryl and C₁₋₈-alkylaryl groupand V is selected from an optionally substituted linear or branchedC₁₋₂₀-alkyl, C₂₋₂₀-alkenyl, C₂₋₂₀-alkynyl group, an aryl group and aC₁₋₂₀-alkylaryl group, sulfide, sulfoxide, sulfone, amine, a polyalkylamine, phosphine or other phosphorous containing group.
 7. The compoundas claimed in claim 6 wherein Z is divalent and selected from oxygen,NR² and NNR²R³ or comprises OH and H, W is selected from OH, OR⁶,O(M^(+n))_(1/n) and NR²R³ and R and R¹ are each selected from anoptionally substituted C₁₋₂₀-alkyl, C₂₋₁₂-alkenyl, C₂₋₁₂-alkynyl, arylC₁₋₈-alkylaryl group and R², R³ and R⁶ are each selected fromC₁₋₄-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, aryl and C₁₋₈-alkylaryl and V isselected from an optionally substituted linear or branched C₁₋₆-alkyl,C₂₋₆-alkenyl and C₂₋₆-alkynyl group and an aryl group.
 8. The compoundas claimed in claim 1 wherein Q is CXYR¹ wherein X and Y are eachselected from hydrogen, —C(O)R, CN or C(O)W and W is selected from OH,OR⁶, O(M^(+n))_(1/n), R and R¹ are, independently, an optionallysubstituted C₁₋₈-alkyl group, R⁶ is a C₁₋₄-alkyl group and M is a metalion selected from a lanthanide, main group or transition metal and V isvinyl, C₁₋₄-alkyl, phenyl or a C₁₋₈-alkylaryl group.
 9. A compound offormula (R⁵O)₃SiCH₂CH₂Q wherein Q is selected from CXYR¹ and —C(Z)Rwherein Z is divalent and selected from oxygen, NR² and NNR²R³ orcomprises OH and H, and wherein X and Y are each selected from —C(Z)R,CN and C(O)W and W is selected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³and R, R¹, R², R³ and R⁶ are each selected from hydrogen and anoptionally substituted linear or branched group selected fromC₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, an aryl andC₁₋₄₀-alkylaryl group and M is a metal ion selected from a lanthanide,actinide, main group or transition metal; n is an integer from 1 to 4and R⁵ is a linear or branched C₁₋₄₀, alkyl group, an aryl orC₁₋₄₀-alkylaryl group.
 10. A compound of formula(R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ wherein Q is selected from CXYR¹ and—C(Z)R wherein Z is divalent and selected from oxygen, NR² and NNR²R³ orcomprises OH and H, and wherein X and Y are each selected from —C(Z)R,CN and C(O)W and W is selected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³and R, R¹, R², R³ and R⁶ are each selected from hydrogen and anoptionally substituted linear or branched group selected fromC₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, an aryl andC₁₋₄₀-alkylaryl group and M is a metal ion selected from a lanthanide,actinide, main group or transition metal; n is an integer from 1 to 4.11. A process for the preparation of a compound as claimed in claim 9,the process comprising the free radical addition of CHXYR¹ to trialkoxyvinyl H₂C═CHSi(OR⁵)₃, where R⁵ is a linear or branched C₁₋₁₂ alkyl, arylor alkylaryl group; in the presence of a free radical initiator.
 12. Aprocess for the preparation of a compound as claimed in claim 1, theprocess comprising the treatment of silica or alumina with a compound offormula (R⁵O)₃SiCH₂CH₂Q, and (R⁵O)₃SiCH(CH₂Q)CH₂CH₂Si(OR⁵)₃ and(R⁵⁰)₃SiV in a solvent.
 13. A process for treating a feedstock of acarbon-carbon bond formation reaction, an oxidation, reduction,alkylation, polymerisation, hydroformylation, arylation, acylation,isomerisation, carboxylation, carbonylation, esterification,trans-esterification or rearrangement reaction, the process comprisingcatalyzing the reaction by using a compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2; such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula
 1. 14. A process for theremoval of or reducing the level of an unwanted organic or inorganiccompound from a liquid substrate, the process comprising contacting saidsubstrate with a compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2; such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula
 1. 15. The processaccording to claim 14 in which the unwanted compound is removed from areaction mixture, waste stream or waste water or bound or attached toother organic compounds.
 16. A process of acid-catalysing a chemicalreaction, the process comprising contacting a feedstock to be subjectedto acid catalysis with a compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2; such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula
 1. 17. A process ofcarrying out a heterogeneously-catalysed reaction selected fromoxidation, reduction, a carbon-carbon bond formation reaction,alkylation, polymerisation, hydroformylation, arylation, acylation,isomerisation, carboxylation, carbonylation, esterification,trans-esterification or rearrangement reaction on a feedstock to besubjected to the said reaction, the process comprising catalyzing thereaction by using a compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2; such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula
 1. 18. A process ofcarrying out a cation or anion exchange reaction with a substratecontaining ions to be exchanged, the process comprising using in theprocess a compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2; such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula 1 with the substrate. 19.A process for immobilising a biological molecule, the process comprisingcontacting said biological molecule with a compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2; such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula
 1. 20. An anti-microbialcomposition comprising a compound of Formula 1:

wherein Q is selected from CXYR¹ and —C(Z)R wherein Z is divalent andselected from oxygen, NR² and NNR²R³ or comprises OH and H, and whereinX and Y are each selected from hydrogen, —C(Z)R, CN and C(O)W and W isselected from OH, OR⁶, O(M^(+n))_(1/n) and NR²R³ and R, R¹, R², R³ andR⁶ are each selected from hydrogen and an optionally substituted linearor branched group selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl,C₂₋₄₀-alkynyl group, an aryl and C₁₋₄₀-alkylaryl group and M is a metalion selected from a lanthanide, actinide, main group or transition metaland V is selected from an optionally substituted linear or branchedgroup selected from C₁₋₄₀-alkyl, C₂₋₄₀-alkenyl, C₂₋₄₀-alkynyl group, anaryl group, a C₁₋₄₀-alkylaryl, sulfide, sulfoxide, sulfone, amine, apolyalkyl amine, a phosphine or other phosphorous containing group; n isan integer from 1 to 4; the free valences of the silicate oxygen atomsare saturated by one or more of: silicon atoms of other groups ofFormula 1, hydrogen, a linear or branched C₁₋₁₂-alkyl group, by endgroups R⁴ ₃M¹O_(1/2), by cross-linking bridge members R⁴_(q)M¹(OR⁵)_(m)O_(k/2), Al(OR⁵)_(3-p)O_(p/2) or R⁴Al(OR⁵)_(2-r)O_(r/2)or by chains comprising (R⁴ _(e)SiO_(f/2))_(g); where M¹ is Si or Ti; eis an integer from 2 to 3 and f is an integer from 1 to 2 such thate+f=4 and g is an integer from 1 to 10⁸; R⁵ is a linear or branchedC₁₋₄₀, alkyl group, an aryl or C₁₋₄₀-alkylaryl group; and R⁴ is a linearor branched C₁₋₄₀-alkyl group, an aryl or C₁₋₄₀-alkylaryl group; k is aninteger from 1 to 3 and q and m are integers from 0 to 2; such thatm+k+q=4; p is an integer from 1 to 3; and r is an integer from 1 to 2;wherein both B and C are always present and a, b, c and d are integerssuch that the molar ratio of b:a+c+d, is from 0.00001 to 100,000, andwherein CXYR¹ and —C(Z)R are monovalent and connected to the rest of thecompound through the carbon atom, and wherein A, B, C, and D designatethe four components of the compound of Formula 1 and a carrier.
 21. Theprocess for the preparation of a compound as claimed in claim 10, theprocess comprising the free radical addition of CHXYR¹ to trialkoxyvinyl silane, H₂C═CHSi(OR⁵)₃, where R⁵ is a linear or branched C₁₋₁₂alkyl, aryl or alkylaryl group; in the presence of a free radicalinitiator.